Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MED. DYNAMICS SATICAN VIDEO CAMERA 5410

K-Number: K843294 · 1984-12-12

Decision Date1984-12-12
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MED. DYNAMICS SATICAN VIDEO CAMERA 5410 is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1984-12-12 under 510(k) number K843294. The device is classified under product code KQM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED. DYNAMICS SATICAN VIDEO CAMERA 5410?

MED. DYNAMICS SATICAN VIDEO CAMERA 5410 is a medical device that received FDA 510(k) clearance on 1984-12-12. The listed applicant is Medline Industries, Inc.. The 510(k) number is K843294.

When did MED. DYNAMICS SATICAN VIDEO CAMERA 5410 receive FDA 510(k) clearance?

MED. DYNAMICS SATICAN VIDEO CAMERA 5410 received FDA 510(k) clearance on 1984-12-12, under 510(k) number K843294.

Who is the listed applicant for MED. DYNAMICS SATICAN VIDEO CAMERA 5410?

The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED. DYNAMICS SATICAN VIDEO CAMERA 5410?

The FDA product code for MED. DYNAMICS SATICAN VIDEO CAMERA 5410 is KQM.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medline Industries, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 223 devices →

Related Devices (Code: KQM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑